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Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT

BACKGROUND: Pituitary adenomas are mostly benign tumors, although certain cases have invasiveness, which might be related with high expression of miR-106b. The PTEN-PI3K/AKT signal pathway is known to be related with cell migration and invasion. Among these, PTEN is the target gene for miR-106b. Whe...

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Autores principales: Zheng, Zhiming, Zhang, Yongchao, Zhang, Zhen, Yang, Yihang, Song, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360419/
https://www.ncbi.nlm.nih.gov/pubmed/28288092
http://dx.doi.org/10.12659/MSM.900092
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author Zheng, Zhiming
Zhang, Yongchao
Zhang, Zhen
Yang, Yihang
Song, Tao
author_facet Zheng, Zhiming
Zhang, Yongchao
Zhang, Zhen
Yang, Yihang
Song, Tao
author_sort Zheng, Zhiming
collection PubMed
description BACKGROUND: Pituitary adenomas are mostly benign tumors, although certain cases have invasiveness, which might be related with high expression of miR-106b. The PTEN-PI3K/AKT signal pathway is known to be related with cell migration and invasion. Among these, PTEN is the target gene for miR-106b. Whether miR-106b affects invasiveness of pituitary adenoma via PTEN-PI3K/AKT is unclear. MATERIAL/METHODS: Both invasive and non-invasive pituitary adenoma tissue samples were collected from our Neurosurgery Department, in parallel with brain tissues after head contusion surgery. Pituitary adenoma cell line HP75 was cultured in vitro and divided into NC and miR-106b inhibitor groups for measuring cell cycle/proliferation. Malignant growth of cells was measured by agarose gel clonal assay, while cell migration and invasion were reflected by starch assay and Transwell assay, respectively. The expression of PTEN, PI3K/AKT, and MMP-9 was measured. RESULTS: MiR-106b was significantly up-regulated in pituitary adenoma but PTEN was down-regulated, especially in invasive tumors. The inhibition of miR-106b remarkably suppressed proliferation and anchorage-independent growth of HP75 cells, with major arrest of cell cycles. The inhibition of miR-106b significantly depressed starch healing and invasive potency of cells. A negative targeted regulation existed between miR-106b and PTEN, as the inhibition of miR-106b significantly enhanced PTEN expression, affecting the activity of downstream PI3K/AKT signaling pathway, thus affecting migration and invasion of pituitary adenoma. CONCLUSIONS: MiR-106b can affect migration and invasion of pituitary adenoma cells via regulating PTEN and further activity of the PI3K/AKT signaling pathway and MMP-9 expression.
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spelling pubmed-53604192017-03-29 Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT Zheng, Zhiming Zhang, Yongchao Zhang, Zhen Yang, Yihang Song, Tao Med Sci Monit Lab/In Vitro Research BACKGROUND: Pituitary adenomas are mostly benign tumors, although certain cases have invasiveness, which might be related with high expression of miR-106b. The PTEN-PI3K/AKT signal pathway is known to be related with cell migration and invasion. Among these, PTEN is the target gene for miR-106b. Whether miR-106b affects invasiveness of pituitary adenoma via PTEN-PI3K/AKT is unclear. MATERIAL/METHODS: Both invasive and non-invasive pituitary adenoma tissue samples were collected from our Neurosurgery Department, in parallel with brain tissues after head contusion surgery. Pituitary adenoma cell line HP75 was cultured in vitro and divided into NC and miR-106b inhibitor groups for measuring cell cycle/proliferation. Malignant growth of cells was measured by agarose gel clonal assay, while cell migration and invasion were reflected by starch assay and Transwell assay, respectively. The expression of PTEN, PI3K/AKT, and MMP-9 was measured. RESULTS: MiR-106b was significantly up-regulated in pituitary adenoma but PTEN was down-regulated, especially in invasive tumors. The inhibition of miR-106b remarkably suppressed proliferation and anchorage-independent growth of HP75 cells, with major arrest of cell cycles. The inhibition of miR-106b significantly depressed starch healing and invasive potency of cells. A negative targeted regulation existed between miR-106b and PTEN, as the inhibition of miR-106b significantly enhanced PTEN expression, affecting the activity of downstream PI3K/AKT signaling pathway, thus affecting migration and invasion of pituitary adenoma. CONCLUSIONS: MiR-106b can affect migration and invasion of pituitary adenoma cells via regulating PTEN and further activity of the PI3K/AKT signaling pathway and MMP-9 expression. International Scientific Literature, Inc. 2017-03-13 /pmc/articles/PMC5360419/ /pubmed/28288092 http://dx.doi.org/10.12659/MSM.900092 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
spellingShingle Lab/In Vitro Research
Zheng, Zhiming
Zhang, Yongchao
Zhang, Zhen
Yang, Yihang
Song, Tao
Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title_full Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title_fullStr Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title_full_unstemmed Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title_short Effect of miR-106b on Invasiveness of Pituitary Adenoma via PTEN-PI3K/AKT
title_sort effect of mir-106b on invasiveness of pituitary adenoma via pten-pi3k/akt
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360419/
https://www.ncbi.nlm.nih.gov/pubmed/28288092
http://dx.doi.org/10.12659/MSM.900092
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